Olney Richard K, Lewis Richard A, Putnam Timothy D, Campellone Joseph V
American Association of Electrodiagnostic Medicine, 421 First Avenue S.W., Suite 300 East, Rochester, MN 55902, USA.
Muscle Nerve. 2003 Jan;27(1):117-21. doi: 10.1002/mus.10317.
At this time, there are no widely accepted criteria for the diagnosis of multifocal motor neuropathy. Furthermore, there is insufficient empirical data to define clinical and laboratory features that may reliably separate certain lower motor neuron syndromes with overlapping features as distinct. The AAEM therefore developed five criteria through a formal consensus process that are described in this document to act as a guide for diagnosing multifocal motor neuropathy with a high level of confidence (definite multifocal motor neuropathy) or with a moderate level of confidence (probable motor neuropathy). In brief, the diagnosis requires clinical weakness without objective sensory loss or upper motor neuron signs in the distribution of two or more named nerves that is due to conduction block in two or more motor nerves outside of common entrapment sites. Furthermore, normal results are required for sensory nerve conduction studies.
目前,对于多灶性运动神经病的诊断尚无广泛认可的标准。此外,也没有足够的经验数据来明确那些能够可靠区分具有重叠特征的某些下运动神经元综合征的临床和实验室特征。因此,美国电诊断医学协会(AAEM)通过正式的共识过程制定了五条标准,本文将对这些标准进行描述,以作为高置信度诊断多灶性运动神经病(确诊的多灶性运动神经病)或中等置信度诊断(可能的运动神经病)的指南。简而言之,诊断需要临床肌无力,在两条或更多命名神经的分布区域内无客观感觉丧失或上运动神经元体征,且这是由常见卡压部位以外的两条或更多运动神经的传导阻滞所致。此外,感觉神经传导研究结果需正常。